Canonical Allele Identifier: PA2827771989
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Trp1801Gly
CA206668
NM_001353951.2:c.5401T>G